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Statistical Programmer Analyst Jobs (NOW HIRING)

Biogen

Sr Analyst, Statistical Programming

Cambridge, MA · On-site

$95K - $130K/yr

Position is based in Durham, NC or in Cambridge, MA About this role The Senior Analyst, Statistical Programming leads and oversees statistical programming activities both internally and externally ...

EDETEK

Senior Statistical Programmer

Edetek is seeking a highly skilled Senior Statistical Programmer to join our dynamic team ... As a leader in data analytics, we are dedicated to providing innovative solutions to our clients in ...

LivaNova

Statistical Programmer II

Boston, MA · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.

LivaNova

Statistical Programmer II

Phoenix, AZ · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.

KG Tiger

Statistical Programmer

Plymouth Meeting, PA

... analyzing very large amounts of data Technical skills/knowledge in one or more of the following ... D. in Statistics, Mathematics or related field with two to five years of experience OR a Bachelor ...

Diverse Lynx

Statistical Programmer

Edison, NJ · On-site

Statistical Programmer Fulltime position available in Edison, NJ - Hybrid. Requires 10 - 25 years ... DPS. • Conduct kick-off meeting • Program and validate all analysis datasets and output in ...

Biogen

NC · On-site

$116K - $163K/yr

This position can be based in Durham, NC or Cambridge, MA About this role The Principal Analyst, Statistical Programming leads and oversees statistical programming activities both internally and ...

Biogen

NC · On-site

$95K - $130K/yr

Position is based in Durham, NC or in Cambridge, MA About this role The Senior Analyst, Statistical Programming leads and oversees statistical programming activities both internally and externally ...

LivaNova

Statistical Programmer II

Raleigh, NC · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.

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Statistical Programmer Analyst information

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$62K

$100.7K

$152.5K

How much do statistical programmer analyst jobs pay per year?

As of Jul 5, 2026, the average yearly pay for statistical programmer analyst in the United States is $100,711.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,000.00 and $126,500.00 per year, depending on experience, location, and employer.

What are Statistical Programmer Analysts?

Statistical Programmer Analysts are professionals who develop, test, and maintain statistical programs for analyzing data, typically in industries such as healthcare, pharmaceuticals, finance, and research. They work closely with statisticians and data managers to ensure data is accurately processed and reported, often using programming languages like SAS, R, or Python. Their responsibilities include creating analysis datasets, generating tables, listings, and figures, and ensuring compliance with regulatory requirements. Statistical Programmer Analysts play a key role in transforming raw data into meaningful insights that support decision-making and research outcomes.

How do Statistical Programmer Analysts typically collaborate with clinical research teams during a study?

Statistical Programmer Analysts work closely with clinical research teams, including biostatisticians, data managers, and clinical project managers, to ensure accurate analysis and reporting of clinical trial data. They are responsible for programming data sets, creating statistical tables, listings, and figures, and validating results to support regulatory submissions or publications. Effective communication and collaboration are essential, as they often attend regular team meetings to discuss requirements, troubleshoot data issues, and ensure timelines are met. This teamwork fosters a dynamic environment where analytical and technical expertise directly contribute to the success of clinical research projects.

What are the key skills and qualifications needed to thrive as a Statistical Programmer Analyst, and why are they important?

To thrive as a Statistical Programmer Analyst, you need strong skills in statistical analysis, programming (especially in SAS, R, or Python), and a relevant degree in statistics, mathematics, or a related field. Familiarity with clinical trial data standards (like CDISC), data management systems, and regulatory submission requirements is often required, along with certifications in SAS or similar tools. Attention to detail, analytical thinking, and effective collaboration are critical soft skills for this role. These skills and qualities are vital to ensure accurate data analysis, regulatory compliance, and successful team-based project delivery in data-driven environments.

What is the difference between Statistical Programmer Analyst vs Data Analyst?

AspectStatistical Programmer AnalystData Analyst
Required CredentialsBachelor's in Statistics, Computer Science, or related field; experience with SAS, R, or PythonBachelor's in Statistics, Data Science, or related field; proficiency in Excel, SQL, and visualization tools
Work EnvironmentPharmaceutical, clinical research, or healthcare industries; focus on programming and statistical analysisVarious industries including finance, marketing, healthcare; focus on data interpretation and reporting
Employer & Industry UsageCommon in clinical trials, biotech, pharma companiesWidely used across multiple sectors including business, finance, and healthcare

The main difference is that a Statistical Programmer Analyst primarily focuses on programming and analyzing clinical or research data using statistical software, while a Data Analyst often handles broader data interpretation and reporting across various industries. Both roles require similar technical skills but differ in industry focus and specific responsibilities.

More about Statistical Programmer Analyst jobs
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Statistical Programmer Analyst jobs near you
Infographic showing various Statistical Programmer Analyst job openings in the United States as of June 2026, with employment types broken down into 33% Full Time, 39% Part Time, and 28% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $100,711 per year, or $48.4 per hour.

Lead Statistical Programmer

Katalyst Healthcares and Life Sciences

Remote

Other

Posted 12 days ago

Job description

Responsibilities:
  • Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs.
  • Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables.
  • Create statistical analysis outputs to be used in support of final reports, abstracts, posters, Manu scripts, and other clinical publications; support systems to produce electronic regulatory submissions.
  • ssist in establishing standardized programming procedures and work instructions.
  • Develop, enhance, evaluate, and validate standardized macros and utility programs to ensure that regulatory requirements are met through validation/compliance activities.
  • Develop and maintain clinical processing workflow systems.
  • ssist in the development of client proposal documents.
  • Provide leadership, project specific training, stakeholder management, external sponsor support, resource management, and project management for the required programming tasks supporting clinical trial activities.
  • Provide input into and negotiate statistical programming timelines. Ensure that timelines are adhered to and coordinate and lead a statistical programming team to successful completion of a study within given timelines and budgets.
  • Trained in sponsor SOPs and disseminate knowledge to project team members as appropriate.
  • Provide input into, and mentor statistical programmers to provide input into documents produced by other functions (e.g., biostatisticians, data managers, medical writers, etc.) records handling (e.g., Chapter 21 of the US Code of Federal Regulation - Part and electronic submission of clinical data to agencies (e.g., e-CTD guidance and CDISC SDTM and ADaM standards).
  • ssist in updating/writing PROMETRIKA standard operating procedures (SOPs).
  • Develop tools in SAS® for data analysis and reporting that comply with regulatory requirements.
  • Develop specifications (e.g., metadata files), annotate CRFs and create SAS® programs for the mapping of raw datasets to CDISC SDTM standards.
  • Create define.xml files from metadata files for SDTM and ADaM.
  • Convert data received in other formats to SAS® datasets.
Requirements:
  • Must have expertise in SAS/BASE, SAS/STAT, and knowledge of SAS/CONNECT, SAS/ACCESS, SAS/MACRO, SAS/GRAPH, SQL, and ODS.
  • Knowledge of SDTM, ADaM, FDA and ICH guidance.
  • Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in computer systems.
  • Good organizational skills across individual projects and managing own and teamwork loads. Ability to organize, manage and complete multiple assignments with challenging timelines independently and effectively.
  • Consistent experience as a lead statistical programmer on several concurrent projects.
  • Strong understanding of drug development, including knowledge of interfaces and interdependencies with other functions.
  • Strong mentoring skills as shown by leadership of projects and if applicable, junior team members.
  • Excellent analytical skills.
  • Proven ability to learn new systems and function in an evolving technical environment.
  • bility to negotiate and influence to achieve results.
  • Good presentation skills.
  • Good business awareness/business development skills (including financial awareness).
  • bility to create, maintain and define strategies to improve the efficiency of running a clinical trial.
  • Work effectively in a quality-focused environment.
  • Knowledge of other programming languages and database management software packages is a plus.

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